Background: Premature senescence occurs in adult hepatobiliary diseases and worsens the
prognosis through deleterious liver remodeling and hepatic dysfunction. Senescence might …

Biliary atresia (BA) is a neonatal liver disease characterized by progressive obstruction and
fibrosis of the extrahepatic biliary tree as well as fibrosis and inflammation of the liver …

The severe acute respiratory syndrome coronavirus 2 pandemic has drastically altered all
facets of clinical care and research. Clinical research in hepatology has had a rich tradition …

To investigate the utility of liver stiffness measurement by shear wave elastography (SWE)
and several commonly used biomarkers in differentiating biliary atresia (BA) from other …

To investigate the mechanism of 25 hydroxyvitamin D (25 (OH) D) deficiency in children with
biliary atresia (BA) and its effect on liver fibrosis. The serum vitamin D and 25 (OH) D, and …

Aims Infants with biliary atresia (BA) are treated with Kasai portoenterostomy (KPE) surgery,
but many BA patients need subsequent salvage liver transplants. The aim of this study is to …

Conclusions: Serum MMP-7 has high discriminative properties to differentiate BA from other
forms of neonatal cholestasis. MMP-7 cutoff values vary according to assay technology …

Serum FGF19 predicts outcomes of Kasai portoenterostomy in b... : Hepatology Serum FGF19
predicts outcomes of Kasai portoenterostomy in biliary atresia : Hepatology AASLD Publications …

Conclusions: These findings identify a key function of the IL-13/IL-4Rα/STAT6 pathway in
ILC2 plasticity and an alternate circuit driven by IL-2 to promote nILC2 stability and …

Advances in microsystem engineering have enabled the development of highly controlled
models of the liver that better recapitulate the unique in vivo biological conditions. In just a …